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Sturge-Weber syndrome Type I: a rare case report. [PDF]
Hendieh B +7 more
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Dyke-Davidoff-Masson syndrome in an 8-year-old child: Report of a case. [PDF]
Bahlouli N +6 more
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Beyond the leptomeningeal angioma: a comprehensive review of MR imaging features of Sturge-Weber Syndrome, from early vascular responses to tissue necrosis. [PDF]
Cerron-Vela CR +2 more
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Uveitis in Parry-Romberg syndrome: A case report and review of literature.
Dutta Majumder P +3 more
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Cephalalgia, 2021
Background Parry-Romberg syndrome is a neuro-cutaneous disease characterized by progressive hemifacial atrophy. Although common, headache in this population is scarcely reported in the literature.
T. Foiadelli +7 more
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Background Parry-Romberg syndrome is a neuro-cutaneous disease characterized by progressive hemifacial atrophy. Although common, headache in this population is scarcely reported in the literature.
T. Foiadelli +7 more
semanticscholar +1 more source
PROGRESSIVE FACIAL HEMIATROPHY
Archives of Neurology & Psychiatry, 1932Originally described by Romberg in 1846, and for this reason likewise known as Romberg's disease, progressive facial hemiatrophy has since aroused the interest of clinicians practically in every part of the world and furnished the theme for a large number of publications.
Nelson K. Fromm
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PROGRESSIVE FACIAL HEMIATROPHY
Archives of Neurology And Psychiatry, 1945An intense and widespread interest has been manifested in the disease described by Parry, in 1825, and by Romberg, in 1846, and named by Eulenburg, in 1871, progressive facial hemiatrophy. In recent years many articles have appeared on this subject in English, German and French. Among these the monographic work of Archambault and Fromm 1 is outstanding.
R. Wartenberg
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